Breast Cancer Clinical Trial

Feasibility and Effectiveness of an Internet-based Intervention to Manage Fatigue in Breast Cancer Survivors

Summary

The purpose of this project is to determine the feasibility and effectiveness of a 6-week, internet-based, Energy Conservation and Activity Management intervention among women who report cancer-related fatigue following breast cancer treatment.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

breast cancer diagnoses
not currently receiving active treatment in the form of chemotherapy or radiation therapy
at least 18 years of age
fatigue severe enough to limit daily activities (score ≥ 4 on 7-point Fatigue Severity Scale)(Krupp, LaRocca, Muir-Nash, & Steinberg, 1989);
functional English fluency and literacy;
Participant has a smart device that operates on the Android or Apple platform
Participant is able to use the Ecological Momentary Assessment application before going to bed every night

Exclusion Criteria:

self-reported history of diagnosis of co-morbidities that have been associated with poor sleep and fatigue: chronic insomnia, chronic fatigue syndrome, unstable heart, lung, or neuromuscular disease, insulin-dependent diabetes, sleep apnea, chronic oral steroid therapy, and night-shift employment,
Disability due to a diagnosis other then breast cancer
Currently taking medication for depression, sleep issues, or fatigue.

Study is for people with:

Breast Cancer

Study ID:

NCT04160182

Recruitment Status:

Withdrawn

Sponsor:

Danielle Mockensturm

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There is 1 Location for this study

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University of Toledo
Toledo Ohio, 43606, United States

How clear is this clinincal trial information?

Study is for people with:

Breast Cancer

Study ID:

NCT04160182

Recruitment Status:

Withdrawn

Sponsor:


Danielle Mockensturm

How clear is this clinincal trial information?

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